| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73828804-73829029 | Common:1; Rare:53 | ||||
| chr2:73892704-73893061 | Common:3; Rare:67 | ||||
| chr2:73986314-73986498 | Rare:26 | ||||
| chr2:74147849-74148140 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178676-74179012 | Common:3; Rare:85 | ||||
| chr2:74374653-74374802 | Rare:30 | ||||
| chr2:74421601-74421771 | Rare:56 | ||||
| chr2:74440419-74440651 | Rare:61 | ||||
| chr2:74458100-74458522 | Common:1; Rare:128 | ||||
| chr2:74459570-74460016 | Rare:143 | ||||
| chr2:74465312-74465421 | Rare:30; Clinvar:1 | ||||
| chr2:74472389-74472762 | Common:4; Rare:173 | ||||
| chr2:74482908-74483385 | Common:2; Rare:180 | ||||
| chr2:74502340-74502624 | Common:1; Rare:59 | ||||
| chr2:74503305-74503475 | Rare:43 |